Dipyridamole Tablet
Product Images NDC 0115-1070

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Dipyridamole (NDC 0115-1070). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal Pharmaceuticals Of New York Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

12 (Dipyridamole Tablets Usp 1)

Chemical structure diagram of Dipyridamole, showing its molecular arrangement with multiple nitrogen-containing rings and hydroxyl groups.*

FDA Label Image

12 (Dipyridamole Tablets Usp 2)

Dipyridamole Tablets, USP 25 mg oral tablets label showing 100 tablets per bottle. The label states the active ingredient and strength, manufacturer Amneal Pharmaceuticals Pvt. Ltd. in India, and distributor Amneal Pharmaceuticals LLC, Bridgewater, NJ. It includes storage instructions, dosage advisory, and a barcode.*

FDA Label Image

12 (Dipyridamole Tablets Usp 3)

Label of Dipyridamole Tablets USP, 50 mg oral tablets, supplied as 100 tablets per bottle by Amneal Pharmaceuticals. The label includes dosage strength, NDC 0115-1071-01, manufacturer information Amneal Pharmaceuticals Pvt. Ltd. (India), distributor Amneal Pharmaceuticals LLC (USA), storage temperature, and a barcode.*

FDA Label Image

12 (Dipyridamole Tablets Usp 4)

Dipyridamole Tablets, USP 75 mg oral tablets in a bottle label from Amneal Pharmaceuticals LLC. The label shows 100 tablets, Rx only, with storage instructions at 20 to 25°C. Manufactured by Amneal Pharmaceuticals Pvt. Ltd. in India, distributed by Amneal Pharmaceuticals LLC, Bridgewater, NJ. Includes a barcode and lot/expiration date area.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.